A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007916



Internal ID18750447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683853..109710508hg38UCSC Ensembl
Innerchr1:110226475..110253130hg19UCSC Ensembl
Innerchr1:110027998..110054653hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3826656
hg1926656
hg1826656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv265n100
Supporting Variantsnssv3494675
Samples
Known GenesGSTM1, GSTM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007916
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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